CFTR

cystic fibrosis transmembrane conductance regulator
OMIM: 602421, Gene2Phenotype

18 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 18 panels
Amber CFTR in Cholestasis Level 2: Gastroenterological disorders Version 1.5 Component of the following Super Panels: Liverome Superpanel	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Cystic fibrosis, MIM# 219700
Green CFTR in Ciliary Dyskinesia Level 2: Respiratory disorders Version 1.63	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert list Phenotypes Cystic fibrosis bronchiectasis
Green CFTR in Congenital Diarrhoea Level 2: Gastroenterological disorders Version 1.23	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Cystic fibrosis, MIM# 219700
Green CFTR in Interstitial Lung Disease Level 2: Respiratory disorders Version 1.2	3 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert list Victorian Clinical Genetics Services Phenotypes Cystic fibrosis, MIM# 219700
Green CFTR in Mendeliome Version 1.3512	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Cystic fibrosis, MIM# 219700 Congenital bilateral absence of vas deferens, MIM# 277180
Green CFTR in Pancreatitis Level 2: Gastroenterological disorders Version 1.6	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Cystic fibrosis
Green CFTR in Pulmonary Fibrosis_Interstitial Lung Disease Level 2: Respiratory disorders Version 0.92	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Cystic fibrosis, MIM# 219700
Green CFTR in Phagocyte Defects Level 2: Immunological disorders Version 1.44 Component of the following Super Panels: Immunological disorders_SuperPanel	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert list Phenotypes Cystic fibrosis, MIM# 219700
Red CFTR in Skeletal dysplasia Level 3: Skeletal dysplasias Level 2: Skeletal disorders Version 0.346	1 review	Not set	Sources Expert Review Green Emory Genetics Laboratory Victorian Clinical Genetics Services
Green CFTR in Mackenzie's Mission_Reproductive Carrier Screening Level 2: Screening Version 0.110	0 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Cystic fibrosis, 219700 (3)
Green CFTR in Additional findings_Paediatric Level 2: Screening Version 0.278	0 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources BabySeq Category A gene Expert Review Green Phenotypes Cystic fibrosis
Green CFTR in Fetal anomalies Version 1.465	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Genomics England PanelApp Phenotypes Cystic fibrosis, MIM# 219700
Green CFTR in Prepair 1000+ Level 2: Screening Version 2.14	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Cystic fibrosis, MIM#219700 MONDO:0009061
Green CFTR in Genomic newborn screening: BabyScreen+ Level 2: Screening Version 1.140	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green BabySeq Category A gene BeginNGS Phenotypes Cystic fibrosis, MIM#219700 Tags treatable respiratory
Green CFTR in Pneumothorax Level 3: Structural lung disorders Level 2: Respiratory disorders Version 1.1	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert list Phenotypes Cystic fibrosis MONDO:0009061
No list CFTR in Transplant Co-Morbidity Level 2: Screening Version 0.20	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert list Phenotypes Congenital bilateral absence of vas deferens MIM#277180 Cystic fibrosis MIM#219700
Green CFTR in Prepair 500+ Level 2: Screening Version 2.0	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Cystic fibrosis, MIM#219700 MONDO:0009061
Green CFTR in Infertility and Recurrent Pregnancy Loss Version 1.50	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Congenital bilateral absence of vas deferens, MIM# 277180